5-Amino-2-methylbenzenesulfonamide → HCID 69291819, compound

HRID 2224525Notes

Reaction equation

HRID 2224525 reaction equation
[F:1][CH:2]([F:25])[C:3]1[N:8]2[N:9]=[CH:10][C:11]([C:12]([OH:14])=O)=[C:7]2[N:6]=[C:5]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][CH:16]=2)[CH:4]=1.[NH2:26][C:27]1[CH:28]=[C:29]([S:34]([NH2:37])(=[O:36])=[O:35])[C:30]([CH3:33])=[CH:31][CH:32]=1>>[CH3:33][C:30]1[CH:31]=[CH:32][C:27]([NH:26][C:12]([C:11]2[CH:10]=[N:9][N:8]3[C:3]([CH:2]([F:25])[F:1])=[CH:4][C:5]([C:15]4[CH:16]=[CH:17][C:18]([C:21]([F:23])([F:24])[F:22])=[CH:19][CH:20]=4)=[N:6][C:7]=23)=[O:14])=[CH:28][C:29]=1[S:34](=[O:36])(=[O:35])[NH2:37]

Participants

3

Procedure

The title compound was prepared from 7-difluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.1) and 3-amino-6-methyl-benzenesulfonamide [CAS-No. 6973-09-7] according to general procedure II. Yellow solid. MS (ISP) 526.2 [(M+H+]; mp 249° C.

Sources & evidence

ORD record
ord-adab4945c33b486989c1036d9a048f80
Source dataset
uspto-grants-2008_05
Patent number
US07378417B2

Reaction notes

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